BEUDAMED
    1,076 results · 23ms · Sources: EU EUDAMED, US FDA

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    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·May 18, 2020

    HEMI HEAD 50MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code KWL·June 24, 2025

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·February 26, 2010

    Medline HOI LUMBAR REF DYNJ902823G Lot 20AKA895 Expiration 2021-05-31 1 each GTIN (01)10193489219180

    FDA Enforcement
    Class II ·Terminated·Medline Industries Inc·March 4, 2020

    Medline HOI LUMBAR REF DYNJ902823G Lot 20AKA895 Expiration 2021-05-31 1 each GTIN (01)10193489219180

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OJH·January 21, 2020

    UNKNOWN TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MEH·March 17, 2017

    STEM: AMISTEM H HA COATED STD STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 6, 2022

    EDITOR'S CHOICE

    FDA Adverse Event
    Malfunction ·UNK·Product code HOI·October 4, 2003

    *

    FDA Adverse Event
    Other ·*·Product code HOI·July 25, 2003

    SEARS OPTICAL

    FDA Adverse Event
    Other ·SEARS OPTICAL MONTCLAIR PLAZA·Product code HOI·July 24, 2003

    READING GLASSES

    FDA Adverse Event
    Malfunction ·BCI·Product code HOI·September 14, 2000

    UNK

    FDA Adverse Event
    Malfunction ·UNK·Product code HOI·September 1, 2000

    FOSTER GRANT 53 (SQUARE) 17-136 PD58 5MM - 2.00 CE

    FDA Adverse Event
    UNK·Product code HOI·December 26, 2017

    BOARD STIFF PROGRESSIVE READERS +250 MAGNIFICATION

    FDA Adverse Event
    Malfunction ·EYEBOBS, LLC.·Product code HOI·December 18, 2025

    REDI-READERS

    FDA Adverse Event
    Other ·MAGNIVISION·Product code HOI·July 7, 2004

    EYEGLASSES NON POLYCARBONATE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code HOI·May 7, 2024

    VERILUX PROGRESSIVE LENSES

    FDA Adverse Event
    Injury ·DR DAVID GEFFEN·Product code HOI·September 27, 2002

    KATE SPADE BRYLIE RNL 135

    FDA Adverse Event
    Malfunction ·COACH SERVICES INC. DBA KATE SPADE C/O SOLUCIONES XB MEXICO, S. DE R.L. DE C.V.·Product code HOI·March 27, 2024

    PLASTIC READING GLASSES FROM THE DOLLAR TREE

    FDA Adverse Event
    Injury ·GREENBRIER INTERNATIONAL·Product code HOI·July 13, 2018

    EYE GLASS

    FDA Adverse Event
    CORRECT OPTICAL·Product code HOI·November 15, 1993